Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
  • A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
  • C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
  • C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
  • C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
  • C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
  • C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
  • C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
  • C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
  • C07C217/84—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
  • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
  • C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
  • C07C275/48—Y being a hydrogen or a carbon atom
  • C07C275/54—Y being a carbon atom of a six-membered aromatic ring, e.g. benzoylureas

Definitions

• R 1 is fluorine and R 2 is fluorine, chlorine or bromine
• R 3 is the radical CH 2 CF 3 , CClFCHClF, CF 2 CHBr 2 , CH(CF 3 ) 2 , CH 2 CF 2 CF 3 or CF 2 CHFCF 3
• R 4 is hydrogen or fluorine
• R 5 is fluorine, chlorine or methoxy.
• Process a) is normally carried out in the temperature range from -10° to +200° C., preferably from 0° to 100° C., e.g. at room temperature, and, if desired in the presence of an organic base, e.g. triethylamine.
• Process b) is carried out in the temperature range from 0° to 150° C., preferably at the boiling point of the solvent employed and, if desired, in the presence of an organic base such as pyridine, and/or with the addition of an alkali metal or alkaline earth metal, preferably sodium.
• process c) i.e.
• a temperature range from about 60° C. to the boiling point of the reaction mixture is preferred, and the solvent employed is preferably an aromatic hydrocarbon such as toluene, xylene, chlorobenzene and the like.
• nitro compounds of formula VII are also novel and constitute an object of the present invention. They can be prepared e.g. by haloalkylating a 2,5-dihalo-4-nitrophenol (q.v. French patent specification 2,005,876) or by reacting 2,5-dihalo-4-fluoronitrobenzene with a haloalkanol in alkaline solution and dimethyl sulfoxide as solvent (q.v. "The Chemistry of the Hydroxyl Group", pp. 83-124; Interscience Publishers Inc., New York, 1971).
• Urethanes of formula VI can be obtained in a manner known per se by reacting a benzoylisocyanate of formula III with a suitable alcohol or by reacting a benzamide of formula V, in the presence of a base, with a corresponding ester of chloroformic acid Cl--COOR.
• the good pesticidal activity of the compounds of formula I of the invention corresponds to a mortality of at least 50-60% of the above pests.
• These compounds also comprise the salts of sulfuric acid esters and sulfonic acids of fatty alcohol/ethylene oxide adducts.
• the sulfonated benzimidazole derivatives preferably contain 2 sulfonic acid groups and one fatty acid radical containing 8 to 22 carbon atoms.
• alkylarylsulfonates are the sodium, calcium or triethanolamine salts of dodecylbenzenesulfonic acid, dibutylnaphthalenesulfonic acid, or of a naphthalenesulfonic acid/formaldehyde condensation product.
• corresponding phosphates e.g. salts of the phosphoric acid ester of an adduct of p-nonylphenol with 4 to 14 moles of ethylene oxide.
• Ready-for-use dusts are obtained by intimately mixing the carriers with the active ingredient.
• the finely ground active ingredient is intimately mixed with the adjuvants, giving a suspension concentrate from which suspensions of any desired concentration can be obtained by dilution with water.
• Each batch of flushed out pupae is counted to determine the toxic effect of the test compound on the maggot development. A count is then made after 10 days of the number of flies which have hatched out of the pupae.
• Cotton plants (about 20 cm high) are sprayed with an aqueous emulsion (obtained from a 10% emulsifiable concentrate) containing 100 ppm of the test compound. After the spray coating has dried, the cotton plants are populated with Spodoptera littoralis and Heliothis virescens larvae in the L 3 -stage. The test is carried out at 24° C. and 60% relative humidity. At 24 hour intervals, a mortality count is made and the larvae are also examined for inhibition of development and moulting.
• aqueous emulsion obtained from a 10% emulsifiable concentrate

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Dentistry (AREA)
• Pest Control & Pesticides (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Agronomy & Crop Science (AREA)
• General Health & Medical Sciences (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• Environmental Sciences (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Applications Claiming Priority (6)

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Cited By (6)

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Citations (7)

Family Cites Families (4)

• 1987
  • 1987-02-23 EP EP91101254A patent/EP0432135A1/de not_active Withdrawn
  • 1987-02-23 ES ES87810100T patent/ES2051770T3/es not_active Expired - Lifetime
  • 1987-02-23 EP EP87810100A patent/EP0235089B1/de not_active Expired - Lifetime
  • 1987-02-23 AT AT87810100T patent/ATE69603T1/de not_active IP Right Cessation
  • 1987-02-23 DE DE8787810100T patent/DE3774590D1/de not_active Expired - Lifetime
  • 1987-02-24 IL IL81662A patent/IL81662A/xx not_active IP Right Cessation
  • 1987-02-26 EG EG111/87A patent/EG18264A/xx active
  • 1987-02-26 CA CA000530631A patent/CA1340467C/en not_active Expired - Fee Related
  • 1987-02-27 AU AU69527/87A patent/AU590911B2/en not_active Ceased
  • 1987-02-27 DK DK102987A patent/DK102987A/da not_active Application Discontinuation
  • 1987-02-27 BR BR8700956A patent/BR8700956A/pt active Search and Examination
  • 1987-02-27 ZW ZW42/87A patent/ZW4287A1/xx unknown
  • 1987-02-28 KR KR1019870001764A patent/KR910000252B1/ko not_active IP Right Cessation
  • 1987-02-28 CN CN198787100956A patent/CN87100956A/zh active Pending
  • 1987-02-28 MY MYPI87000210A patent/MY101880A/en unknown
• 1990
  • 1990-11-30 JP JP2341220A patent/JPH0669994B2/ja not_active Expired - Fee Related
• 1991
  • 1991-02-13 US US07/656,108 patent/US5132325A/en not_active Expired - Fee Related
  • 1991-11-29 GR GR91401606T patent/GR3003236T3/el unknown
• 1992
  • 1992-12-10 DK DK148892A patent/DK148892A/da not_active Application Discontinuation

Patent Citations (7)

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